A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations

Title
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations
Authors
Keywords
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Journal
MOVEMENT DISORDERS
Volume 24, Issue 3, Pages 441-445
Publisher
Wiley
Online
2009-01-02
DOI
10.1002/mds.22435

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